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Methanol → 3-methoxy-1-((6-methylpyridin-3-yl)methyl)-4-nitro-1H-indazole

HRID 79467
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HRID 79467 반응식
I[C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[N+:11]([O-:13])=[O:12])[N:4]([CH2:14][C:15]2[CH:16]=[N:17][C:18]([CH3:21])=[CH:19][CH:20]=2)[N:3]=1.N1C2C(=CC=C3C=2N=CC=C3)C=CC=1.[F-].[K+].[CH3:38][OH:39]>C1(C)C=CC=CC=1.[Cu](I)I>[CH3:38][O:39][C:2]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[N+:11]([O-:13])=[O:12])[N:4]([CH2:14][C:15]2[CH:16]=[N:17][C:18]([CH3:21])=[CH:19][CH:20]=2)[N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 887MethanolHCID 13181,10-PhenanthrolineHCID 522689Potassium FluorideHCID 672608103-iodo-1-((6-methylpyridin-3-yl)methyl)-4-nitro-1H-indazole

생성물 1

HCID 672596893-methoxy-1-((6-methylpyridin-3-yl)methyl)-4-nitro-1H-indazole수율 66%

시약·촉매·용매 2

HCID 83717
Copper iodide
촉매
HCID 1140Toluene용매

실험 절차

A mixture of 3-iodo-1-((6-methylpyridin-3-yl)methyl)-4-nitro-1H-indazole (0.520 g, 1.32 mmol), 1,10-phenanthroline (0.238 g, 1.32 mmol), copper iodide (0.251 g, 1.32 mmol) and potassium fluoride (40% on alumina) (1.05 g, 7.26 mmol) in methanol (2.7 mL) and toluene (13 mL) was purged with argon and heated at reflux for 14 hours. After cooling, the mixture was filtered through glass fiber filter paper, concentrated under reduced pressure and purified by silica gel chromatography (5-25% EtOAc in hexanes) to give 3-methoxy-1-((6-methylpyridin-3-yl)methyl)-4-nitro-1H-indazole (0.260 g, 66% yield) as a brown gum.

후처리

  1. customwas purged with argon
  2. temperatureheated
  3. temperatureat reflux for 14 hours
  4. temperatureAfter cooling
  5. filtrationthe mixture was filtered through glass fiber
  6. filtrationfilter paper
  7. concentrationconcentrated under reduced pressure
  8. custompurified by silica gel chromatography (5-25% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-c949dc8c7c4e42afa506852d6723aed0
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08841455B2

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